Srikrishna, A and Rao, Srinivasa M (2004) The First Total Synthesis of the Antimicrobial Sesquiterpenes (±)-Enokipodins A and B. In: Synlett, 2 . pp. 374-376.
Full text not available from this repository. (Request a copy)Abstract
Efficient first total synthesis of antimicrobial sesquiterpenes enokipodins A and B (1 and 2, respectively) and formal total synthesis of cuparene-1,4-diol (5) and cuparene-1,4-quinone (7) have been accomplished starting from 2,5-dimethoxy-4-methylacetophenone employing Claisen rearrangement and ring-closing metathesis reaction as key steps.
| Item Type: | Journal Article |
|---|---|
| Publication: | Synlett |
| Publisher: | Thieme |
| Additional Information: | The copyright belongs to Thieme. |
| Keywords: | Sesquiterpenes;enokipodins A and B;Ring;Cosing metathesis;Claisen rearrangement |
| Department/Centre: | Division of Chemical Sciences > Organic Chemistry |
| Date Deposited: | 27 May 2006 |
| Last Modified: | 27 Aug 2008 12:03 |
| URI: | http://eprints.iisc.ac.in/id/eprint/6984 |
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